HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (R)-N5-(Cbz)-N2-(Diphenylacetyl)-(S)-N-(2-hydroxy-1-phenylethyl)-ornithine amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (R)-N5-(Cbz)-(S)-N-(2-hydroxy-1-phenylethyl)ornithine amide hydrochloride | HCID 131722057 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-N5-(Cbz)-N2-(Diphenylacetyl)-(S)-N-(2-hydroxy-1-phenylethyl)-ornithine amide | HCID 86755916 | 129.6% |
Reaction Steps
Prepared according to the method described in Example 1(d) above from (R)-N5 -(Cbz)-(S)-N-(2-hydroxy-1-phenylethyl)ornithine amide hydrochloride (2.0 g, 4.74 mmol; from step (b) above), 2-nitrophenyl diphenyl acetate (1.67 g; 5.21 mmol; see Example 1(c) above) and triethylamine (0.726 mL; 5.21 mmol) in 150 mL of CH2Cl2. The reaction mixture was heated to reflux for 1 hour, followed by standard aqueous work up, yielding 1.78 g of the sub-title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127414 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-af2781fbe18643e18859699589a4afe9 |
| Source note | uspto-grants-2000_10 |